Correlating Heterogeneities in Support Fragmentation to Polymer Morphology in Metallocene-Based Propylene Polymerization Catalysis

IF 3.9 3区 化学 Q2 CHEMISTRY, PHYSICAL ChemCatChem Pub Date : 2024-10-27 DOI:10.1002/cctc.202401183
Joren M. Dorresteijn, Dr. Roozbeh Valadian, Dr. Yuntao Ji, Dr. Silvia Zanoni, Dr. Koen W. Bossers, Dr. Nikolaos Nikolopoulos, Dr. Virginie Cirriez, Dr. Alexandre Welle, Dr. Daniel Curulla-Ferré, Prof. Eelco T.C. Vogt, Prof. Florian Meirer, Prof. Bert M. Weckhuysen
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Abstract

In the field of olefin polymerization catalysis, metallocenes are heterogenized with methylaluminoxane onto silica supports to yield active catalysts. During olefin polymerization, these silica supports act as a framework to control the fragmentation stage, thereby influencing the final polymer product and preventing reactor fouling and fines formation. This study investigates the influence of different silica supports induced on the final polymer product. To study a broad range of silica supports from an industrial silica database, we utilize a hierarchical clustering method to cluster the supports based on their physical properties. From the clustering method, five supports representing the clusters and an industrial benchmark were analyzed at different polymerization stages using focused ion beam–scanning electron microscopy (FIB–SEM) and microcomputed tomography (microCT). This combined FIB-SEM/microCT methodology revealed differences in both fragmentation behavior and polymer morphologies based on structural features, including macropores, mesopores, spray-dried shells, spray-dried spheres, and denser shells. The heterogeneity and ideal fragmentation behavior was further assessed by calculating the replication factor of each support, indicating that silica materials containing macropores and spray-dried shells have an almost ideal replication phenomenon. This multiscale analysis revealed new understanding of catalyst fragmentation for different supports. This understanding could in the future be further developed by the addition of more supports or additional analysis of the supports to the industrial database.

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在茂金属基丙烯聚合催化中,载体破碎的非均质性与聚合物形态的关系
在烯烃聚合催化领域,金属茂烯与甲基铝氧烷在二氧化硅载体上异相化,得到活性催化剂。在烯烃聚合过程中,这些二氧化硅支撑体作为框架来控制裂解阶段,从而影响最终的聚合物产品,防止反应器结垢和细颗粒的形成。本研究考察了不同的二氧化硅载体对最终聚合物产物的影响。为了研究工业二氧化硅数据库中广泛的二氧化硅支撑,我们利用分层聚类方法根据其物理性质对支撑进行聚类。从聚类方法出发,利用聚焦离子束扫描电子显微镜(FIB-SEM)和微计算机断层扫描(microCT)分析了代表聚类的五个支点和一个工业基准在不同聚合阶段。结合FIB-SEM/microCT方法揭示了基于结构特征的聚合物破碎行为和形态的差异,包括大孔、中孔、喷雾干燥壳、喷雾干燥球和致密壳。通过计算各载体的复制因子,进一步评价了其非均质性和理想破碎行为,表明含有大孔和喷雾干燥壳的二氧化硅材料具有近乎理想的复制现象。这种多尺度分析揭示了不同载体催化剂破碎的新认识。今后可以通过增加更多的支持或对工业数据库的支持进行更多的分析来进一步发展这种理解。
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来源期刊
ChemCatChem
ChemCatChem 化学-物理化学
CiteScore
8.10
自引率
4.40%
发文量
511
审稿时长
1.3 months
期刊介绍: With an impact factor of 4.495 (2018), ChemCatChem is one of the premier journals in the field of catalysis. The journal provides primary research papers and critical secondary information on heterogeneous, homogeneous and bio- and nanocatalysis. The journal is well placed to strengthen cross-communication within between these communities. Its authors and readers come from academia, the chemical industry, and government laboratories across the world. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and is supported by the German Catalysis Society.
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